Stridor
Symptom Information:
| Symptom ID: | HPO:0010307 | ||||
| Synonyms: |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Stridor(HPO:0010307) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Upper respiratory tract disorders (excl infections)(MedDRA:10046304) Laryngeal spasm, oedema and obstruction(MedDRA:10023855) Stridor(HPO:0010307) |
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| Database Frequency: | 19 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Acetazolamide-responsive myotonia | (Orphanet:99736) |
| Autosomal dominant Charcot-Marie-Tooth disease type 2C | (Orphanet:99937) |
| BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
| Beta-mannosidosis | (Orphanet:118) |
| Congenital laryngeal web | (Orphanet:2374) |
| D,L-2-hydroxyglutaric aciduria | (Orphanet:356978) |
| Frontometaphyseal dysplasia | (Orphanet:1826) |
| Hurler syndrome | (Orphanet:93473) |
| Laryngeal abductor paralysis | (Orphanet:2808) |
| Maternally-inherited Leigh syndrome | (Orphanet:255210) |
| Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
| Myotonia fluctuans | (Orphanet:99734) |
| Myotonia permanens | (Orphanet:99735) |
| PELIZAEUS-MERZBACHER DISEASE | (OMIM:312080) |
| Potassium-aggravated myotonia | (Orphanet:612) |
| Riboflavin transporter deficiency | (Orphanet:97229) |
| Scheie syndrome | (Orphanet:93474) |
| Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
| Van den Ende-Gupta syndrome | (Orphanet:2460) |